Nickel-catalyzed Kumada cross-coupling reactions of tertiary alkylmagnesium halides and aryl bromides/triflates.

ABSTRACT: We report a Ni-catalyzed process for the cross-coupling of tertiary alkyl nucleophiles and aryl bromides. This process is extremely general for a wide range of electrophiles and generally occurs with a ratio of retention to isomerization >30:1. The same procedure also accommodates the use of aryl triflates, vinyl chlorides, and vinyl bromides as the electrophilic component.

SUBMITTER: Joshi-Pangu A 

PROVIDER: S-EPMC8036247 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature